KR102256757B1 - Polymerase Chain Reaction System - Google Patents

Abstract

The present invention relates to a system structure capable of real-time detection of nucleic acid extraction and amplification reactions and amplified products in a device implementing a polymerase chain reaction. The nucleic acid of the biological sample is used as a medium through a nucleic acid extraction reagent stored therein. Or additionally mixed with the polymerase reaction dried product to form a PCR preliminary mixture and inserted into the nucleic acid extraction cartridge to connect a flow path, and the nucleic acid solution or PCR preliminary extracted from the nucleic acid extraction cartridge A PCR plate receiving the mixture and dispersing it in at least one reaction well containing a dried primer/probe, or a PCR reaction product including a primer/probe, and disposed on the PCR plate, and the reaction well (W A temperature control module including a pair of heating blocks for applying different temperatures adjacent to) and a scanning module disposed under the PCR plate to scan the concentration of the amplified reactants in the reaction well (W). It consists of including.

Description

Polymerase Chain Reaction System

The present invention relates to a system structure capable of real-time detection of extraction and amplification reactions and amplified products of nucleic acids in a device implementing a polymerase chain reaction.

Point of care (POC) diagnosis technology that accurately and quickly diagnoses a patient's disease regardless of time and place is attracting attention as a very important technology for evidence-based precision medicine. On the basis of disease symptoms such as cough, diarrhea, high fever, and genital abnormalities, all infectious pathogens that cause disease symptoms are examined in a short time at a time to identify the causative agent and prescribe optimal antibiotics and treatments. As a key new technology for future precision medicine, many studies are being added and developing. Such on-site diagnosis technology has the advantage of making quick and accurate diagnosis even by non-professionals in the field, such as a pregnancy test kit for confirming pregnancy and a blood glucose meter that can check blood sugar. At present, molecular diagnosis technology has developed multiple test methods that can simultaneously test various pathogens, and by utilizing these technologies, the exact cause of infectious diseases is known and the optimal prescription is possible, thereby treating the disease early to dramatically improve the recovery period of the patient. It is gaining attention as a core technology of future medicine that improves the quality of medical care by shortening it to and reduces medical costs.

However, the current molecular diagnosis system takes more than 3 hours to confirm the results and must be used by experienced experts, so for the POC molecular diagnosis required in the field, the complex nucleic acid extraction process and real-time gene amplification test can be fully automated. It is essential to develop a compact device that has been developed, and it must be able to operate easily even if it is not a professional person.

As a representative molecular diagnosis method, there is a method using a polymerase chain reaction (PCR (polymerase chain reaction), hereinafter referred to as'PCR'). Polymerase chain reaction (PCR) was invented by Kary Mullis in 1985 and can amplify specific DNA quickly and easily, so it is widely used in molecular biology and molecular diagnostics. Using PCR/RT-PCR, it is possible to check whether a specific DNA/RNA exists in a biological sample, so it is widely used to diagnose pathogenic microbial infections such as viruses. As this PCR/RT-PCR technology evolves into realtime PCR (quantitative PCR), the results can be seen at the end of PCR, thus simplifying the test process and significantly reducing the test time, as well as accurately quantifying the number of pathogens. It is used as a standard diagnostic method to monitor the therapeutic effects of HIV, HCV, and HBV viruses. In addition, it is used as the most important technology for diagnosing diseases as it can test gene expression patterns or genetic mutations related to specific diseases.

In order to perform such PCR, a nucleic acid extraction step of removing substances that inhibit PCR reaction from a biological sample and extracting pure nucleic acid is required. The nucleic acid extraction process consists of multiple steps, and requires skilled technology to manipulate biological samples and nucleic acid extraction, and if it is done manually, there is a contamination problem due to operator's error, so most of the molecular diagnosis is performed using automated nucleic acid extraction equipment. have.

Since a real-time quantitative PCR device must be equipped for PCR reaction and detection of reaction products, molecular diagnosis has been performed mainly in large hospitals or specialized clinical laboratory institutions.

Through recent research and development, various automated systems and devices using the same have been developed to automate the entire process of nucleic acid extraction, PCR reaction, and reaction product detection, so that PCR can be easily used even without specialized technology.

However, existing devices are too expensive or take a lot of processing time, and it is difficult to perform various tests at once.

To explain the basic principle of PCR, the DNA double helix is heated to 95 degrees to separate it into a single strand, and then the reaction solution is cooled to an annealing temperature to selectively use complementary primers at both ends of the site to be amplified in the PCR reaction solution. When hybridization is performed, the DNA polymerase repeats a reaction to form a double helix by sequentially connecting four kinds of nucleotide triphosphates complementary to each single strand of A, G, T, and C. Experimentally, heating and cooling the PCR reaction solution are repeatedly performed 30 to 45 cycles (n) to amplify a ^{specific DNA double helix by 2 n exponentially.} The RT-PCR reaction was extended as a method for detecting RNA by synthesizing cDNA through reverse transcription and then amplifying it through PCR.

In order to fully utilize PCR for molecular diagnosis, the newly developed real-time quantitative PCR principle is explained. For quantitative analysis of the amplified DNA using PCR reaction, a substance that generates fluorescence in proportion to the amount of DNA is PCR After adding to the reaction solution, fluorescence is measured in each cycle to find the cycle in which the critical fluorescence value is detected, and from this, the concentration of the initial target nucleic acid is quantitatively measured.

Since the invention of PCR, while various application technologies have been developed, numerous pathogens and disease-related gene sequences have been known through the genome project, and molecular diagnosis that amplifies these disease-related DNA/RNA sequences to diagnose qualitatively and quantitatively has rapidly developed. come. Since conventional PCR takes around 2 hours to cycle through the temperature, methods for performing PCR more quickly and accurately for on-site diagnosis have been continuously developed. (Lab Chip, 2016, 16, 3866-3884)

In order to perform the PCR reaction in a short time, the temperature of the reaction solution must be changed rapidly. In addition, in order to amplify only the desired target through an accurate PCR reaction, the primers must be designed to specifically attach to the desired target, and the annealing temperature must be accurately controlled in the PCR temperature cycle reaction.

For this, compared to the 0.5 and 0.2 ml reactors that are commonly used in laboratories. Micro-PCR reaction vessels with small heat capacity and good heat transfer as possible have been developed. Since these microreactors use less reaction solution and have a large surface area, heat transfer is possible quickly and rapid heating and cooling are possible. A silicon wafer with a size of 17 X 15 mm, 10 ul of PCR solution was put in a thin reaction groove of 40-80 um and covered with a glass plate to keep the surface area high (>100 mm2/10ul), but the conventional Peltier thermal block was used. Thus, it did not show that one cycle shortened the time to about 3 minutes (Clin. Chem. 40/9, 1815-1818 (1994)).

In order to rapidly thermally cycle the PCR reactor, a method of repeatedly immersing the PCR reactor in a high-temperature water bath and a low-temperature water bath was developed as an initial PCR reaction device. (Turbo Thermalcycler. Bioneer Corp. Daejeon). The PCR equipment that circulates the reactor in the different temperature zones has the advantage of being able to quickly and accurately perform PCR reactions by immersing the reactor in a constant temperature water tank in which the temperature is accurately maintained in advance as a space movement method. However, since several constant temperature water tanks are required, the equipment is large and maintenance is laborious, and the PCR equipment adopting the time difference temperature circulation method that changes the temperature over time using a Peltier element in a fixed block is the main type.

The PCR method using micro-channels was also developed as a space-moving temperature circulation method and a time difference temperature circulation method. The space moving temperature circulation method can be broadly divided into an open reactor method that continuously flows in a FIFO (First-In-First-Out) method and a closed type method that repeatedly moves other temperature sections. The open method was developed by Nakano et al. in 1994 by winding a capillary tube around a cylindrical block having compartments with different temperatures and continuously flowing the PCR solution thereto. (Biosci. Biotech. Biochem., 58(2), 349-352, 1994) This is a micro-channel type PCR equipment that repeatedly flows through high and low temperature sections in 1998. It was confirmed that PCR proceeded by passing through 20 cycles with a cycle of 4.5 seconds. (Science 280 1046-1048, 1998)

Korean Patent Publication No. 10-2016-0067872

Therefore, the main object of the present invention is to extract nucleic acids from biological samples, perform PCR reactions, and perform detection of target nucleic acids fully automatically through scanning excitation light and corresponding fluorescence of various wavelengths. It is to provide a device that can be used, is easy to use, and can obtain accurate results in a particularly fast time.

Further, another object of the present invention is to enable rapid and accurate PCR by allowing rapid and repetitive application of the temperature control process required for the PCR process to the temperature required for the heat denaturation process and the exact temperature required for the bonding process, It is to provide a device that can maximize the reliability of the reaction.

As a means for solving the above-described problem, in embodiments of the present invention, as shown in FIGS. 1 to 23, a nucleic acid extraction cartridge for extracting the nucleic acid of the biological sample through a nucleic acid extraction reagent stored therein. (100); At least one reaction in which the nucleic acid extraction cartridge is coupled in a structure in which a flow path is connected, and the nucleic acid solution extracted from the nucleic acid extraction cartridge 100 is applied, and a primer or a primer/probe or a PCR mixture dried product containing a primer probe is accommodated. PCR plate 200 accommodated in the well; And a pair of heating blocks 310 and 320 disposed above the PCR plate 200, applying different temperatures adjacent to the reaction well W, and capable of horizontal operation and vertical movement operation. It is possible to provide a polymerase chain reaction system including the temperature control module 300.

According to an embodiment of the present invention, extraction of nucleic acids from biological samples, PCR reactions, excitation light of various wavelength bands, and real-time reaction product detection through corresponding fluorescence scanning can be automated and performed, and various tests can be performed with a single operation. It is possible to provide a device that is easy to use and can obtain accurate results in a particularly fast time.

In addition, according to an embodiment of the present invention, the temperature control required for the PCR process can be quickly applied to the reaction object at once in real time by controlling the temperature required for the heat denaturation step and the combination of the reaction. There is an effect that can maximize reliability.

In other words, in the case of the conventional temperature control method in which the reaction solution is moved and the temperature is increased, the temperature cannot be uniformly increased, which is disadvantageous to the PCR reaction, and the reaction solution moves and sequentially increases the temperature. By eliminating the problem of high possibility for other reactions to occur because it is not possible to achieve temperature uniformity across the entire reactant at the same time, the temperature range set in the heating block is maintained at a constant temperature, and the temperature is increased by directly pressurizing the entire reaction solution. The temperature increase required for the reaction can be implemented very efficiently.

Furthermore, in the process of changing the temperature from high temperature to low temperature, in order to minimize the time delay, block-shaped heating block structures are arranged side by side, and when the PCR plate is pressed, the positions of the heating blocks are changed individually. Since the heating block having a different temperature is pressed in real time, the problem caused by the required time delay in the temperature change process can be remarkably solved.

Furthermore, by implementing the PCR plate into the nucleic acid extraction cartridge in an insert-type structure, the nucleic acid extraction cartridge is used in common, and the PCR plate used for various test kits is stored in a small space, and a suitable PCR plate is inserted and used as needed. I can. It is possible to analyze up to 6 fluorescence values in one reaction well provided in the PCR plate, and if necessary, the reaction well of the PCR plate can be increased to 8, so that it may be included in the patient's biological sample related to symptoms. All possible pathogens can be amplified and detected, enabling symptom-based multi-molecular diagnostic tests to be provided.

In addition, according to an embodiment of the present invention, the constant temperature plate is divided into regions having a gradient between the first temperature and the second temperature, and a set temperature corresponding to the temperature of the heating block when the heating block is pressed through a driving module By moving the region having 1 temperature or the second temperature) to correspond to each other and performing contact pressurization on the upper and lower surfaces of the PCR plate at the same time, there is also an effect of realizing twice the efficiency compared to the constant temperature plate method maintained at a single temperature. .

In addition, in the implementation of a movable constant temperature plate structure, a sliding tape can be used to secure the reliability of the product configuration and movement as a configuration in which the driving operation is performed, and a method that is implemented at the same time when the heating time of the plate in the target is increased. Since it takes, the advantage of reducing the inspection time by 1/2 is also implemented.

1 is a block diagram showing the configuration of the main parts constituting the polymerase chain reaction system according to an embodiment of the present invention.
2 to 7 are views for explaining the structure of the temperature control module 300 in the present invention.
Figure 8 shows an embodiment of the PCR plate 200 applied to the present invention.
9 to 12 are conceptual diagrams for explaining the structure and operation of the constant temperature plate and the horizontal movement driving module applied to the present invention.
13 is a perspective conceptual diagram of the nucleic acid extraction cartridge of the present invention, showing a structure in which the above-described PCR plate is inserted and coupled.
14 is an exploded perspective view of FIG. 13.
FIG. 15 shows the internal structure of the cartridge lid part R1 in the structure of FIG. 14.
FIG. 16 is a perspective view showing the combined state of the structure of FIG. 14.
17 to 19 show a lower operating state of the cartridge structure of the present invention.
20 shows the overall structure and arrangement of the apparatus constituting the polymerase chain reaction system of the present invention described above.
FIG. 21 is an enlarged view of an arrangement of main parts of the present invention in FIG. 20, and FIG. 22 is a conceptual diagram showing a vertical cross-sectional view of the part of FIG.
FIG. 23 is a side perspective cross-sectional conceptual view of FIG. 22.

Advantages and features of the present invention, and a method of achieving them will become apparent with reference to the embodiments described below in detail together with the accompanying drawings. However, the present invention is not limited to the embodiments described herein and may be embodied in other forms. Rather, the embodiments introduced herein are provided so that the disclosed content may be thorough and complete, and the spirit of the present invention may be sufficiently conveyed to those skilled in the art.

The terms used in the present application are only used to describe specific embodiments, and are not intended to limit the present invention. Singular expressions include plural expressions unless the context clearly indicates otherwise. In the present application, terms such as "comprise" or "have" are intended to designate the presence of features, numbers, steps, actions, components, parts, or combinations thereof described in the specification, but one or more other features. It is to be understood that the presence or addition of elements or numbers, steps, actions, components, parts, or combinations thereof, does not preclude in advance the possibility of the presence or addition.

1 is a block diagram showing the configuration of the main components constituting the polymerase chain reaction system (hereinafter referred to as'the present invention') according to an embodiment of the present invention.

Referring to Figure 1, the polymerase chain reaction system according to an embodiment of the present invention (hereinafter, referred to as'the present invention') is a temperature control process required for the PCR process, the temperature required for the heat denaturation process and the bonding process. Accurate PCR is possible by applying the exact temperature required for (annealing) to the reaction object in real time without time difference, and to maximize the reliability of the reaction, contact the PCR reaction plate to set a specific temperature. It characterized in that it comprises a temperature control module implemented as a heating block structure to be applied.

The temperature control module according to the present invention minimizes the time delay required to implement a temperature from a first temperature to a relatively low temperature second temperature or a second temperature to a relatively high temperature first temperature in the reverse process. Thus, by changing the positions of the heating blocks respectively set to the first temperature and the second temperature, the PCR reaction plate is pressurized in real time, so that the problem due to the required time delay in the temperature change process can be drastically solved. .

Further, in the present invention, it may be implemented to further include a constant temperature plate structure that is disposed under the PCR plate and operates in a horizontally moving structure in a sliding manner. In this case, it is a constant temperature plate structure that maintains the temperature of the PCR plate at the first temperature or the second temperature, thereby minimizing the time required for application of the temperature change condition to maximize the reaction speed.

Specifically, the present invention, the nucleic acid extraction cartridge 100 for extracting the nucleic acid of the biological sample through the medium of the nucleic acid extraction reagent stored therein, forming a PCR preliminary mixture or template, and inserted into the nucleic acid extraction cartridge Combined in a connected structure, receiving the PCR preliminary mixture or template extracted from the nucleic acid extraction cartridge 100, dispersing in at least one reaction well containing at least one of the primers and probes and receiving A temperature control module including a PCR plate 200, a pair of heating blocks 310 and 320 disposed on the PCR plate 200 and applying different temperatures adjacent to the reaction well W ( 300) can be configured including.

The present invention provides the convenience of allowing nucleic acid extraction to be freely performed by inserting a desired sample through the nucleic acid extraction cartridge through the above-described configuration, and at the same time, the temperature cycle required for amplification applied to the PCR plate 200 By using a heating block structure that can directly apply a target temperature to the reaction solution in the PCR plate through a thin film and compression, fast and precise temperature control can be achieved.

In addition, the polymerase chain reaction (hereinafter referred to as'PCR') implemented as a single system so that the detection of the reactants can be performed by scanning the excitation light of various wavelength bands and the corresponding fluorescence under the PCR plate in real time through the scanning module. You can make it possible to provide a device.

2 to 7 are views for explaining the structure of the temperature control module 300 in the present invention.

2 and 3 are perspective conceptual diagrams of the temperature control module of the present invention.

2 and 3, the temperature control module 300 extracts a nucleic acid from a biological sample, mixes it with a polymerase, and receives a PCR (polymerase chain reaction) preliminary mixture or a nucleic acid extract from a nucleic acid extraction cartridge. It performs a function of performing a constant temperature control for the PCR plate 200.

Specifically, the temperature control module 300 has a first pressure surface G1 corresponding to the surface of the reaction well W implemented on the PCR plate 200, and is thermally denatured by a heating unit. It includes a first heating block 310 maintained at a temperature set in the range of the required temperature (hereinafter,'first temperature'). At the same time, the first heating block 310 is disposed to be spaced apart from the corresponding position, a second pressing surface G2 corresponding to the reaction well surface is provided, and a temperature required for annealing by the heating unit ( Hereinafter, it is configured with a second heating block 320 maintained at a temperature set in the range of'second temperature'). In particular, the structures of the first heating block 310 and the second heating block 320 may be implemented to enable horizontal and vertical movements.

In a preferred embodiment, the first heating block 310 and the second heating block 320 have a three-dimensional structure, and may be provided with a flat pressure surface on the lower surface, and the first heating block ( 310) and the second heating block 320 may be disposed to be spaced apart from each other, and each may have a temperature in a different temperature range.

Specifically, the first heating block 310 and the second heating block 320 are arranged to face each other in a structure facing each other, as shown in FIGS. 2 and 3, and a pressing function of a flat structure on the top surface as a whole. It is implemented as a structure for performing, and the upper portion may be provided in a three-dimensional structure of a rectangular parallelepiped. The implementation of the three-dimensional structure of a rectangular parallelepiped is an example, and any shape having a flat-shaped pressing surface for pressing will be included in the gist of the present invention.

In addition, the first heating block 310 and the second heating block 320 are disposed sideways, and adjacent surfaces are implemented in a structure that is spaced apart from each other, and each may be maintained to have a different set temperature.

For example, the first temperature of the first heating block 310 is a temperature applied to the heat denaturation step of separating double-stranded DNA (including DNA extracted from a biological sample), and may be set in the range of 94 to 96°C. I can. In a preferred embodiment of the present invention, it can be maintained at 95 ℃.

Further, the second temperature of the second heating block 320 is a temperature required for annealing of the primers to bind the separated template DNA, and may be set in the range of 50 to 65°C. In a preferred embodiment of the present invention, it can be maintained at 55 ℃.

The first heating block 310 and the second heating block 320 are implemented in a structure including a metal body having a large heat capacity and good heat transfer efficiency, not a method of accommodating water or a heat transfer fluid therein. It can be maintained at the set temperature at all times by the heating unit of. To this end, the heating unit must be controlled through temperature control so that a temperature sensor is installed inside to maintain a constant temperature.

That is, when the PCR preliminary mixture is injected into the PCR plate 200, the first heating block 310 moves horizontally and is adjacent to the surface of the PCR plate 200 when the application of the first temperature is required. do. That is, the first pressing surface (G) is a flat plate structure with a flat structure, and it is possible to heat the entire surface of the PCR plate 200 at the same time at the same temperature and at the same pressing force, allowing uniform temperature transfer to the entire sample. It is done.

In addition, when it is necessary to apply the second temperature required for the bonding step, the second heating block 320 moves horizontally and is located on the top of the PCR plate. Make it possible to heat by pressing force.

In other words, it does not require a separate time to prepare the set temperature reaction, and it is driven in a manner that allows heating with the same pressing force at the same temperature at the same time on the entire surface of the PCR plate 200 by a simple horizontal operation. Compared to the method for controlling the reaction, it is possible to derive a quick and precise PCR reaction.

In addition, since the first heating block 310 and the second heating block 320 are set to different temperatures, the second heating block may be constantly heated by the first heating block by radiant heat or conduction heat. In consideration of this, a cooling fan unit 340 capable of implementing a cooling effect may be provided in the spaced space between the two structures.

It is important that the second heating block 320 relatively maintains a second temperature, such as an annealing temperature of 55° C., minimizing the thermal interference of the first heating block 310 and easily cooling the excess heat. A diverging type cooling pattern that can be radiated by the unit may be provided on the top. For this example, in the present invention, the second heating block 320 may further include a temperature control pattern part 321 implemented on the side of the second pressing surface G2. The temperature control pattern part 321 has a structure in which a plurality of protruding patterns are implemented on the top, and it is possible to increase the heat dissipation efficiency by increasing the contact surface area with air, thereby advantageously maintaining a constant low temperature.

Unlike the method of moving a reaction sample implementing a PCR reaction or moving to another heating zone through a time setting, the present invention has a heating block structure so as to increase a uniform temperature overall and at the same time while the reaction sample is fixed. By applying, it is possible to implement accurate transfer of the first temperature and the second temperature.

In addition, it is preferable that the first heating block 310 or the second heating block 320 in the present invention interlock with the driving module 330 that implements a horizontal operation or a vertical movement operation. The driving module 330 includes guide members 331 and 332 passing through the first heating block 310 and the second heating block 320, and the first heating block 310 and the second heating block 320 It may be to perform the vertical movement along the guide members (331, 332).

That is, in the present invention, the first heating block 310 and the second heating block 320 are disposed to be spaced apart from each other, and according to the operation of the driving module 330, they cross each other to implement vertical movement. Furthermore, by further including an elastic member (S1, S2) disposed under the guide members (331, 332), when the heating blocks (310, 320) pressurize the PCR plate (200), a buffer by giving an appropriate elastic force It is desirable to be able to act (see Fig. 5).

In addition, in the embodiment of the present invention, it is possible to further include a thermostat plate 350 interlocking with the temperature control module described above.

In addition, in the embodiment of the present invention, it is possible to further include a thermostat plate 350 interlocking with the temperature control module described above.

The constant temperature plate 350 is disposed under the structure of the heating blocks 310 and 320 constituting the temperature control module 300, as shown in FIGS. 2 and 3, and the PCR plate 200 enters After that, when the first heating block 310 or the second heating block 320 of the temperature control module 300 presses the PCR plate by horizontal motion and vertical movement, the first heating block 310 or The second heating block 320 can function to have the same temperature as the temperature.

To this end, the constant temperature plate 350 may be configured to further include a horizontal movement driving module 400 that horizontally moves to the lower portion of the PCR plate 200.

To this end, the constant temperature plate 350 may be configured to further include a horizontal movement driving module 400 that horizontally moves to the lower portion of the PCR plate 200.

The horizontal movement driving module 400, as shown in Figs. 2 and 3, a moving bar 420 and a driving motor unit 410 coupled to one end of the constant temperature plate 350, and the driving motor unit ( It may be configured to include a conversion plate 430 for converting the rotational force of the 410 to the horizontal moving force of the moving bar 420.

The horizontal movement driving module 400 allows the constant temperature plate 350 to be horizontally moved in the lower direction of the temperature control module 300 described above. In particular, the constant temperature plate 350 according to an embodiment of the present invention , It may be implemented in a structure divided into a first region heated to a first temperature and a second region heated to a second temperature spaced apart from the first region (refer to the description of FIGS. 21 to 23).

In particular, in a preferred embodiment of the present invention, the temperature control module 300 and the constant temperature plate 350 may be implemented integrally with each other through the guide members 331 and 332.

That is, when the horizontal movement driving module 400 is driven, the temperature control module 300 including the constant temperature plate 350 and the heating blocks 310 and 320 may be moved together.

In this case, the constant temperature plate 350 includes a first region heated to a first temperature and a second region heated to a second temperature spaced apart from the first region, and the first heating block 310 The first pressure surface (G1) of is arranged to correspond to the upper portion of the first region, and at the same time, the PCR plate 200 is placed between the constant temperature plate 350 and the heating blocks 310 and 320 at the same temperature above and below. It can be made to be pressurized.

That is, in the embodiment of the present invention, the constant temperature plate 350 is divided into regions having a gradient between the first temperature and the second temperature, and when the heating block is pressed through the horizontal moving drive module 400, the heating block is By moving horizontally in a sliding structure so that a region having a set temperature (first temperature or second temperature) corresponding to the temperature corresponds to the upper and lower surfaces of the PCR plate, contact pressure is simultaneously performed, thereby allowing the constant temperature plate method to be maintained at a single temperature. Compared to this, it realizes twice the efficiency.

FIG. 4 is a cross-sectional view of the temperature control module in FIG. 3 as viewed from the rear, and FIG. 5 is a cross-sectional view of the temperature control module as viewed from the front.

As described above, the temperature control module 300 of the present invention includes a driving module 330 that implements a horizontal operation or an up-down movement operation of the first heating block 310 and the second heating block 320. It makes it possible to automate the operation of the module.

2 to 5, the driving module 330 performs an operation of moving the first heating block 310 and the second heating block 320 up and down, and at the same time, the horizontal movement driving module 400 Is a portion in contact with the surface of the reaction well on the PCR plate 200 by horizontally moving the first heating block 310 and the second heating block 320, the first pressing surface G1 or the second pressing Make it possible to change it to face (G2).

The first heating block 310 and the second heating block 320 are arranged side by side while being spaced apart from each other, and guide grooves 312 and 322 (refer to FIG. 2) are provided in a through structure. The heating block 310 and the second heating block 320 are seated on the guide members 331 and 332 passing through the guide grooves 312 and 322. Through this, the first heating block 310 and the second heating block 320 move up and down along the guide members 331 and 332 and can press the PCR plate 200 from the top.

Of course, in this case, a constant temperature plate 350 is disposed under the first heating block 310 and the second heating block 320, and the temperature is the same as the first temperature or the second temperature provided by each heating block. Corresponds to the regions having a, so that the PCR plate can be pressed from the top and bottom.

As described above, the temperature control module 300 in the present invention has the advantage of being able to directly apply the first temperature and the second temperature to the entire PCR plate surface to the entire PCR object in the PCR plate 200. , It is possible to realize excellent effects in terms of application speed and reaction efficiency.

In addition, the structure of the heating block of the temperature control module 300 is located at an upper portion that can be moved horizontally at all times and descends only when it is pressed against the PCR plate.

In order to implement such a structure, it is possible to include a first elastic member (S1) having a restoring force that is disposed inside the driving frame so that it always rises upward when it is not compressed. In the present invention, a second elastic member 335 for transmitting a pressing force to prevent application of excessive pressing force is provided in case of implementing pressing in contact with the PCR plate 200 (FIG. 5). In the illustrated embodiment, the second elastic member 335 is implemented as a plate spring structure, and when the first and second heating blocks in the downward direction are pressed, they exert a certain buffering force, and an excessive pressing force is applied to the PCR plate surface. You can control it so that it does not happen.

In addition, in the system structure of the present invention, the PCR plate 200 has a shape of a plate-shaped structure in which a reaction well is implemented on an upper surface. In this case, the PCR plate 200 has a constant temperature, such as a second temperature (ex: 55). ℃) to maintain the range of the lower portion of the thermostatic plate 350 to be configured to further include a structure.

This is a case in which the temperature is increased by intimate contact with the first heating block of the first temperature (ex: 95°C) by the temperature control module 300 of the present invention, or the second temperature is increased by the second temperature (ex: 55°C). This is because when the heating block is in close contact, the internal amplification efficiency is much better only when the PCR plate 200 reaches the target temperature quickly.

Therefore, in the embodiment of the present invention, it is disposed under the PCR plate 200, so that the temperature of the PCR plate 200 to be maintained at the second temperature to be configured to further include a constant temperature plate 350 It is desirable to do it.

Particularly, it is good to implement the constant temperature plate 350 in a manner that is mounted in a fixed type and applies a constant temperature, but as described above, the constant temperature plate 350 itself is partitioned to provide the first temperature and It is more preferable to divide it into a region to which the second temperature is applied, and to implement a structure in which the constant temperature plate can be moved horizontally.

6 is a view showing a state in which the constant temperature plate 350 is horizontally moved to the bottom of the temperature control module through the horizontal moving drive module 400 in the structure of FIG. 2, and FIG. 7 is a constant temperature plate in the operation of FIG. It shows the appearance of changing the temperature range by horizontally moving (350) outward.

That is, in the structure of FIG. 6, when the first heating block 310 is arranged to apply the first temperature, the first region of the constant temperature plate 350 moves horizontally to the bottom of the PCR plate together with the first heating block. Is arranged, the first heating block 310 corresponds to face the upper surface of the PCR plate, and then, as shown in FIG. 7, the second region is horizontally moved to the lower part of the PCR plate together with the second heating block and arranged. In this case, the second heating block is moved horizontally and is operated so as to face the upper surface of the PCR plate.

The horizontal movement operation of the constant temperature plate 350 may be implemented in a sliding manner, and may be implemented to move in contact with a sliding tape that contacts a side portion of the constant temperature plate 350.

Further, referring to FIGS. 6 and 7, this is a conceptual diagram showing the bottom of the temperature control module according to the present invention. As shown, the constant temperature plate 350 includes the PCR plate 200 and the scanning module ( Not shown: The light of the scanning module 500 is arranged between the reference numerals 500 of FIG. 1 and is transmitted to the PCR plate 200 by irradiating the excitation light irradiated from the scanning module and detects fluorescence. A plurality of guided light transmitting portions H may be provided in a through structure.

Accordingly, in the present invention, the nucleic acid extraction, PCR process, and detection process can be implemented in one system with an integrated system equipped with the above-described scanner, and a separate PCR plate structure can be implemented so as to be applicable to various disease diagnosis. .

Figure 8 shows an embodiment of the PCR plate 200 applied to the present invention.

Referring to FIG. 8 and referring to the conceptual diagrams of FIGS. 2 and 3 described above, the PCR plate 200 according to the present invention includes at least one reaction well (W1.. ..Wn) is implemented and the body part 210, extending from one end of the body part 210, is coupled in a structure interpolated to the nucleic acid extraction cartridge 100.

In particular, it may be implemented in a structure in which an insertion part 220 having an injection hole h1 into which the PCR preliminary mixture is injected so as to be introduced from the nucleic acid extraction cartridge 100 is implemented. In addition, the PCR plate 200 has a structure in which a connection part 230 having a flow path part 231 provided on the surface of the body part so as to be connected to the injection hole h1 and connected to the plurality of reaction wells is provided. So that it can be implemented.

Specifically, the PCR plate 200, as shown in Fig. 8, includes a body portion 210 in which a plurality of reaction wells (W1....Wn) are implemented. In this case, in the case of the reaction well, in the illustrated structure, it is implemented as a structure including eight reaction wells, but is not limited thereto, and of course, it can be implemented as a structure having at least one or more. The structure may also be implemented in a concave pattern structure by processing the surface of the body part 210.

In particular, in a preferred embodiment of the present invention, as shown in FIG. 8, a partition wall pattern 215 that partitions a constant region of the reaction well is provided in a protruding structure as shown in FIG. 8. The primer provided in a dried state in the inside and the PCR (polymerase chain reaction) preliminary mixture injected from the nucleic acid extraction cartridge are dispersed and mixed in the reaction well.

In addition, the PCR plate 200 includes a cover member (not shown) that seals the upper portions of the plurality of reaction wells, and the cover member may be formed of a transparent film material having light transmission properties. .

When the cover member is in close contact with the surface of the reaction well to realize the inside of the reaction well as a cavity, the PCR (polymerase chain reaction) premix injected from the nucleic acid extraction cartridge later pushes the air layer present in the upper cavity and inside the reaction well. Will be injected.

Particularly, in the present invention, as in the structure of FIG. 8, a flow path part 231 connected to the reaction well in the body part 210 may be provided. The flow path part is implemented to extend to the distal end 232 of the body part via the body part 210 at a time 231 connected to the injection hole h1, and opposite to the insertion part at the distal part 232 It can be implemented so as to be connected to each of the end of the plurality of reaction holes in the direction to be.

That is, as shown in FIG. 2, when the nucleic acid extraction cartridge is injected through the injection hole h1 provided under the insertion part, the flow path is implemented in a direction x1 crossing the body at the time point 231 of the flow path, It can be implemented to be branched left and right at the distal point of the body and connected to the inlet to each reaction well. The reason for forming the flow path is that a small amount of air layer exists inside the reaction well area sealed by the cover member, so that the injected PCR (polymerase chain reaction) premix is formed at the center line of the body as shown in the structure of FIG. Based on ), it rises from the lower region Cb, and the air layer is pushed up to the upper region Ca of the body.

Therefore, the mixture to be subjected to the PCR reaction is relatively arranged in the lower region (Cb) of the reaction well, which means that the area where the heating block of the present invention performs pressurization and the area that performs detection of the scanner module are shown in FIG. 8 due to the characteristics of the equipment. Likewise, since it is performed in the lower region Cb, it is possible to increase both the precision of detection, the efficiency of the PCR reaction, and the efficiency of the temperature control.

In addition, in the present invention, the PCR plate 200 is preferably made of a synthetic resin material having high light transmittance. This is to improve detection efficiency by using a material having high light transmittance according to the function of the scanner module described above.

Transparent PP. Various synthetic resin materials such as PE, PPA, PMMA, PC, etc. can be applied, but are not necessarily limited thereto, and any material that can secure a certain light transmittance can be applied.

However, the PCR plate 200 can maintain a constant temperature by a heat source applied from the lower constant temperature plate, and one of the PCR (polymerase chain reaction) premix or nucleic acid solution and dried primers and probes filled in the reaction well. For the efficiency of maintaining the temperature of the temperature control module directly applied to the PCR reaction product including at least one side, the thickness of the body 210 may be implemented in a range of 1.0mm to 3.0mm. If the thickness is less than 1.0mm, the high-temperature heat that sets the first temperature is easily transferred to the lower part of the body, resulting in heat interference with the constant temperature plate, making it difficult to control the temperature, and if it exceeds 3.0mm, it is accommodated in the reaction well. It is easy to control the temperature of the material to be formed, but it is difficult to control the temperature of the lower constant temperature plate, and thus it is difficult to maintain a constant temperature.

That is, in the present invention, as described above with reference to FIGS. 4 and 5, the first pressing surface in contact with the surface of the reaction well by horizontally moving the first heating block 310 and the second heating block 320 (G1) or the second pressing surface (G2) is pressed in a structure in contact with the upper surface of the partition wall pattern 215 and the cover member covering the partition wall pattern, and the set temperature is set to a first temperature or a second temperature. The temperature of the reactants is controlled.

In addition, in the case of circulating the temperature for the PCR plate 200, in the temperature control module according to the structure of FIGS. 2 and 3, the first heating block moves horizontally to face the upper surface of the PCR plate in order to raise it to the first temperature. The lower surface of the PCR plate is subjected to contact pressure by moving the first heating block downward after the first region of the constant temperature plate moves horizontally together with the first heating block. The upper surface moves horizontally to face the second heating block, and on the lower surface of the PCR plate 200, the second area of the constant temperature plate moves horizontally together with the second heating block, and then the second heating block moves downward. Thus, the contact is pressurized, and the PCR plate 200 is driven to simultaneously heat and cool the upper and lower surfaces of the PCR plate 200. In the present invention, since the constant temperature plate 350 and the first and second heating blocks 310 and 320 are integrally moved horizontally, the upper and lower pressures of the PCR plate 200 are simultaneously implemented at the same temperature. Of course it can be.

Due to this operation, by performing contact pressurization on the upper and lower surfaces of the PCR plate at the same time, it is possible to implement twice the efficiency compared to the constant temperature plate method maintained at a single temperature, so that when the heating time of the plate in the target is increased, it is simultaneously implemented. By taking the method, the advantage of reducing the inspection time by half is realized.

9 to 12 are views for explaining in detail the structure and operation method of the constant temperature plate and the horizontal moving drive module.

9 shows a structure in which the constant temperature plate 350 is seated in FIGS. 2 and 3, and FIG. 10 shows a structure in which only the constant temperature plate structure is separated.

9 and 10, the constant temperature plate 350 according to an embodiment of the present invention is disposed under the heating block structure constituting the temperature control module shown in FIGS. 2 and 3, and the PCR plate 200 After is placed, when the first heating block 310 or the second heating block 320 of the temperature control module 300 presses the PCR plate by horizontal motion and vertical movement, the first heating block (310) or the second heating block (320) to be able to function to have the same temperature as the temperature.

The constant temperature plate 350, as shown in FIG. 9, is a spacer (Ss) that divides the first region (a1) maintaining a first temperature and the second region (a2) maintaining a second temperature. ) Is provided, and is implemented in a structure in which the first region a1 and the second region a2 are connected with respect to both side ends a3 and a4 of the spacer Ss.

Connector structures (Ca, Cb) are mounted at one end of the constant temperature plate 350 so as to apply power or transmit a control signal.

In particular, the horizontal movement operation of the thermostatic plate 350 is implemented in a sliding manner, and is implemented to move in contact with a sliding tape that contacts the side surface of the thermostatic plate 350 to achieve simplification of the structure as well as mobility. Make it possible to improve.

In this case, a light transmitting part H may be provided in the second area a2 to transmit the detection light of the scanning module 500 that scans the concentration of the amplified reactant.

Temperature sensors Sa and Sb may be provided in the first area a1 and the second area a2 to measure and control the temperature of the corresponding area.

FIG. 11 shows the lower surface of FIG. 10, in which connection connectors (Cc, Cd) for applying control signals and power are provided, and temperature sensors (Sa, Sb) are provided to provide a constant temperature of the first temperature and the second temperature. Make it possible to implement maintenance.

To maintain the temperature of the first region or the second region of the constant temperature plate, a method of mounting various means such as various heating means, heating wires or heating resistors inside the plate may be used, but in a preferred embodiment of the present invention, epoxy printing Implement an electrode and a temperature sensor circuit on the circuit, apply a heating paint between the electrodes, and then attach the metal plates corresponding to the first and second regions to each of the temperature sensors and the heating paint to achieve this effect. .

12 is a conceptual top plan view illustrating the operation method described above in FIGS. 6 and 7 in more detail.

In the present invention, the constant temperature plate 350 to the lower portion of the PCR plate 200 may be configured to further include a horizontal movement driving module 400 that moves horizontally.

The horizontal movement driving module 400, as shown in Figs. 2 and 3, a moving bar 420 and a driving motor unit 410 coupled to one end of the constant temperature plate 350, and the driving motor unit ( It has been described above that it may be configured to include a conversion plate 430 for converting the rotational force of the 410 to the horizontal moving force of the moving bar 420.

As shown in Fig. 12, the nucleic acid extraction cartridge is inserted into the nucleic acid extraction cartridge and combined in a structure in which the flow path is connected, and the nucleic acid solution extracted from the nucleic acid extraction cartridge 100 is injected into the injection hole h1, and the injected nucleic acid The solution is then transferred to the PCR plate 200, which is injected into at least one reaction well in which the dried PCR mixture containing at least one of the primers and probes is accommodated.

Thereafter, the first heating block 310 or the second heating block 320 of the temperature control module 300 of the present invention for forming a first temperature or a second temperature in the reaction well portion of the PCR plate 200 It will descend.

In this case, the horizontal movement driving module 400 horizontally moves the constant temperature plate 350 and the temperature control module 300 together, and the PCR plate is interpolated between the constant temperature plate 350 and the temperature control module 300. It will be arranged in a structure that can be used.

When the heating block horizontally moved through the horizontal movement driving module 400 presses the PCR plate, a first region of the constant temperature plate having a set temperature (first temperature or second temperature) corresponding to the temperature of the heating block, or The second area is arranged to correspond naturally.

That is, when the first region (a1) of the constant temperature plate 350 is horizontally moved to the lower portion of the PCR plate 200 and disposed, the first heating block (Figs. 2 and 310) is moved horizontally at the same time, and the It corresponds to face the upper surface of the PCR plate, and then the heating block descends to come into contact with the upper surface of the PCR plate.

In addition, when the second area (a2) is horizontally moved to the bottom of the PCR plate, the second heating blocks (eh 2, 320) are simultaneously moved horizontally to correspond to the upper surface of the PCR plate. Then, the heating block descends and comes into contact with the upper surface of the PCR plate.

In short, in the case of circulating the temperature of the PCR plate 200, in order to raise the temperature to the first temperature, the first heating block is moved horizontally to face the upper surface of the PCR plate, and the lower surface of the PCR plate is the first region of the constant temperature plate. After moving, the first heating block moves downward to drive the contact pressure.

In addition, in order to lower the temperature back to the second temperature, the upper surface of the PCR plate 200 is horizontally moved to face the second heating block, and on the lower surface of the PCR plate 200, the second region of the constant temperature plate is horizontally moved. After that, the second heating block is moved downward and contact is pressurized, so that simultaneous heating and cooling are performed on the upper and lower surfaces of the PCR plate 200.

In this way, by performing contact pressurization on the upper and lower surfaces of the PCR plate at the same time, it is possible to realize twice the efficiency compared to the constant temperature plate method maintained at a single temperature.

Hereinafter, a nucleic acid extraction cartridge 100 implementing a polymerase chain reaction (PCR) preliminary mixture including a nucleic acid extract on the PCR plate according to the present invention will be described with reference to FIGS. 13 to 19.

13 is a perspective conceptual diagram of the nucleic acid extraction cartridge of the present invention, showing a structure in which the above-described PCR plate is inserted and coupled. FIG. 10 is an exploded perspective view of FIG. 9 and FIG. 11 is a diagram illustrating an internal structure of the cartridge cover R1 in the structure of FIG. 10. (In this example, the structure of the gene amplification plate having two reaction wells will be described.)

13 to 15, the nucleic acid extraction cartridge 100 according to the present invention is a cartridge having a plurality of partition wall structure receiving portions 22, 23, 24, 25, 26 containing a solution required for DNA extraction. Includes a cartridge body portion (R2) coupled to the cover portion (R1) and the cover portion (R1) in an insertion structure, and provided with a reaction receiving portion (11) for reacting or washing a solution introduced from the receiving portions with a sample It can be configured.

In this case, a piston part 18 for injecting the PCR premix purified by the reaction receiving part 11 into the injection hole h1 of the PCR plate 200, which is combined in a structure that is interpolated into the cartridge body part R2. ).

The operation of the present invention will be described with reference to FIGS. 14, 15, and 17 of the nucleic acid extraction cartridge. FIG. 16 is a transparent perspective view of FIG. 13 showing the internal structure after being combined.

The nucleic acid extraction cartridge of the present invention is equipped with a rotary valve 19 having a flow path 19-1 formed therein on the bottom surface of the body portion R2, and when the rotary valve is rotated, each of the cartridge body R2 is accommodated. The space of the parts 11, 12, 13, 14, 15, 16, 17 and the flow path of the rotary valve 19 may be connected. It is designed to connect a flow path to a specific receiving unit and then operate the piston 18 to take a solution contained in the receiving unit and transfer the material to another receiving unit or PCR plate 200.

As shown in Figs. 14 and 15, the cartridge cover (R1) has a receiving portion (22, 23, 24, 25, 26) containing each solution required for DNA extraction is formed, the receiving portion The bottom surface is sealed with a film or the like, so it is designed to be easily pierced by a penetrating needle (composition 10-1 in FIG. 12). In addition, five holes 21-1, 21-2, 27, 28, and 29 are formed.

The first receiving part 22 of the cartridge cover part R1 has a Binding buffer, the second receiving part 23 has a 1st Washing buffer, the third receiving part 24 has a 2nd Washing buffer, and the fourth receiving part 25 In the 3rd washing buffer, the fifth receiving part 26 contains the elution buffer.

The PCR plate 200 is covered with a film made of a transparent plastic material [polyethylene, polypropylene, PET, etc.], and a PCR mixture including at least one of the dried PCR primers and probes is contained inside the reaction well. It is the same as the structure described above in 8.

The action of the nucleic acid extraction cartridge of the present invention may proceed in the following order.

1. Input of biological samples

The cartridge body portion (R2), the cartridge cover portion (R1) and the PCR plate 200 are mounted in an automated equipment to be described later in a combined state, and a biological sample (blood ) Is injected.

2. Nucleic acid leakage from cells and binding to beads

As shown in FIG. 17, the Binding buffer of the first receiving unit 22 through the rotation of the rotary valve 19 disposed under the cartridge body unit R2 and the action of the piston 18 is transferred to the reaction receiving unit ( 11) and mixed with biological samples and beads of magnetic tablet (MT) (magnetic beads coated with silica).

The magnetic tablet (MT) used in the present invention is a magnetic tablet (MT) mounted on the end of the through-pipe extending into the reaction receiving portion 11 of the cartridge body portion (R2), the cells contained in the biological sample The nucleic acid extracted from the magnetic tablet is dissolved and the surface of the dispersed magnetic bead and the nucleic acid bind to each other.

In this case, instead of the magnetic tablet, the magnetic beads may be suspended in a Binding buffer and used.

Thereafter, when a sonication tip is inserted into the sealed second hole 21-2 of the cartridge body R2 and the ultrasonic wave is applied, the ultrasonic wave is transmitted through the plastic and the biological sample, the tablet, and the binding buffer are mixed and reacted. The liquid is homogenized, and at this time, the biological tissues contained in the biological sample are also crushed so that the nucleic acid is leaked, and the leaked nucleic acid is bound to the surface of the beads.

When a magnetic bar is inserted into the third hole 27 of the cartridge body R2, the bead is fixed to the wall of the reaction receiving unit, and the remaining reaction solution is transferred to the first receiving unit through the rotation of the rotary valve and the action of the piston. Is transferred.

3. 1st washing

The 1st Washing buffer of the second receiving unit 23 is introduced into the reaction receiving unit 11 through the rotation of the rotary valve of the cartridge body unit R2 and the action of the piston shown in FIG. 16 to mix the nucleic acid-bound beads. .

Thereafter, when the magnetic bar is removed from the third hole 27 of FIG. 14 and ultrasonic waves are applied to the sonication tip to the second hole 21-2, the first cleaning is performed. Due to this primary washing, substances that are non-specifically bound to the beads other than nucleic acids are washed.

The magnetic bar is inserted into the third hole 27 so that the bead is fixed to the wall of the reaction receiving unit, and the primary washing liquid is transferred to the second receiving unit 23 through the rotation of the rotary valve and the action of the piston.

4. Second washing

The 2nd washing buffer of the third receiving unit 24 is introduced into the reaction receiving unit 11 through the rotation of the rotary valve of the cartridge body R2 and the action of the piston shown in FIG. 16 to mix the nucleic acid-bound beads. .

Thereafter, when the magnetic bar is removed from the third hole 27 of FIG. 14 and ultrasonic waves are applied to the sonication tip to the second hole 21-2, secondary cleaning is performed. Due to this secondary washing, substances that are non-specifically bound to the beads other than nucleic acids are washed.

The magnetic bar is inserted into the third hole 27 so that the bead is fixed to the wall of the reaction receiving unit, and the secondary washing liquid is transferred to the third receiving unit 24 through the rotation of the rotary valve and the action of the piston.

5. 3rd washing

The 3rd washing buffer of the fourth receiving unit 25 is introduced into the reaction receiving unit 11 through the rotation of the rotary valve of the cartridge body unit R2 and the action of the piston shown in FIG. 16 to mix the nucleic acid-bound beads. .

Thereafter, when the magnetic bar is removed from the third hole 27 of FIG. 14 and ultrasonic waves are applied to the sonication tip to the second hole 21-2, the third cleaning is performed. Due to this third washing, substances that are non-specifically bound to the beads other than nucleic acids are washed.

The magnetic bar is inserted into the third hole 27 so that the bead is fixed to the wall of the reaction receiving unit, and the third washing liquid is transferred to the fourth receiving unit 25 through the rotation of the rotary valve and the action of the piston.

6. Nucleic acid elution

The elution buffer of the fifth receiving unit 26 is introduced into the reaction receiving unit 11 through the rotation of the rotary valve of the cartridge body R2 shown in FIG. 16 and the action of the piston, and mixed with the bead to which the nucleic acid is bound.

Thereafter, when the magnetic bar is removed from the third hole 27 of FIG. 14 and a sonication tip is inserted into the second hole 21-2 and ultrasonic waves are applied, the nucleic acid bound to the bead surface is dissolved in the elution buffer. .

7. PCR premix generation

A magnetic bar is inserted into the third hole 27 so that the bead is fixed to the wall of the reaction receiving unit, and the elution buffer in which the nucleic acid is dissolved is introduced into the sixth receiving unit 17 by rotating the rotary valve and selecting a small piston. Then, it is mixed with the PCR material (a mixture of polymerase, dNTP, etc.) contained in the sixth receiving part, thereby producing a PCR premix. The'PCR premix' used in the present invention is defined and used as embodied by the above materials. The above process is omitted when the PCR reaction product including at least one of the primers and probes is dried in each well of the PCR plate, and the nucleic acid eluate is directly injected into the PCR plate as follows.

8. Transfer to PCR plate

The PCR premix generated in the sixth receiving portion through the rotation of the rotary valve of the cartridge body portion R2 shown in FIG. 16 and the action of the piston is introduced into the PCR plate 200, and the primer contained in the PCR plate 200 And at least one of the probes and mix. As shown in FIG. 19, the injection process moves through the flow path Y of the rotary valve by pressurization of the piston 18 and is injected into the injection port h1.

Thereafter, a heating rod is inserted into the fourth hole 29 so that the cover film at the inlet portion of the PCR reaction plate is heated under pressure, thereby sealing the PCR reaction plate.

9. PCR reaction

Finally, the PCR plate 200 contains at least one of nucleic acids extracted from biological samples, polymerase, dNTP, primers and probes, and other buffers.

Therefore, the PCR reaction is performed through the application of pressurized heat through the temperature control module of the present invention described above to the PCR plate 200.

20 to 23 show the overall structure and arrangement of the apparatus constituting the polymerase chain reaction system of the present invention described above.

As shown in Figure 20, when the nucleic acid extraction cartridge 100 is mounted inside the polymerase chain reaction system according to the present invention, the above-described PCR plate 200 is seated on the side. The portion where the reaction well corresponding to the body portion of the PCR plate 200 is present is exposed to the outside, and the temperature control module 300 described above is disposed thereon.

FIG. 21 is an enlarged view of an arrangement of main parts of the present invention in FIG. 20, and FIG. 22 is a conceptual diagram showing a vertical cross-sectional view of the part of FIG. FIG. 23 is a side perspective cross-sectional conceptual view of FIG. 22.

21 to 23, the PCR preliminary mixture containing the nucleic acid extracted from the inside of the nucleic acid extraction cartridge 100 according to the present invention is injected into the PCR plate 200 in which the reaction well is implemented. A first pressing surface G1 corresponding to the reaction well surface is implemented on the upper part of the PCR plate 200, and a first heating block 310 maintained at a temperature required for thermal denaturation by a heating unit is provided. The second heating block 320, which is disposed in a horizontal manner, and can be implemented in a structure in which a region to be pressed is changed is disposed adjacently. Accordingly, the PCR preliminary mixture injected into the reaction well is directly heated by the heating block in accordance with the first temperature (95° C.) required for thermal denaturation or the second temperature (55° C.) required for annealing.

In addition, as shown in FIGS. 22 and 23, a constant temperature plate 350 is disposed under the PCR plate 200 to maintain the temperature of the PCR plate 200 at a constant temperature level.

A scanning module 500 is disposed under the constant temperature plate 350, so that the light L irradiated by the light irradiation unit E1 passes through the light transmitting portion H of the constant temperature plate 350, and the PCR plate ( 200) is reached and fluorescence detection is performed.

In an embodiment of the present invention, as described above, when the temperature is increased by contacting the first heating block of the first temperature (ex: 95°C) by the temperature control module, or the second temperature (ex: 55°C) When the second heating block of) is in close contact, if the PCR plate 200 is maintained in a certain temperature range, temperature control of the internal amplification reaction becomes much easier, so that the temperature of the above-described constant temperature plate is kept constant at the second temperature. Maintaining this is a very important factor to increase the reliability of the reaction. When the temperature of the PCR plate is raised to 95℃, the temperature of the PCR plate is increased by increasing the heat transfer rate by making the first temperature block and the first constant temperature zone in close contact with each other. It can quickly reach 95°C in 2-3 seconds.

When performing RT/PCR for detecting an RNA target, use a PCR premix or PCR plate containing the RT-PCR reaction dry matter. The low-temperature block may be adjusted to an RT reaction temperature, adhered to the PCR reaction plate, and maintained for as long as the RT reaction time, and then the PCR reaction may be performed after performing a reverse transcription reaction.

The presence or absence of the amplified nucleic acid or the concentration of the amplified nucleic acid can be determined through the PCR reaction and this information can be used for diagnosis. At this time, the presence or concentration of the amplified nucleic acid can be achieved using a conventional nucleic acid detection method. have.

For example, a method of using SYBR green, a DNA minor grove-inserted fluorescent dye, which is a DNA intercalation dye, a method of scanning excitation light in various wavelength bands and corresponding fluorescence using a probe with various fluorescence and quencher attached, etc. May be used, but is not limited thereto.

In the above, the present invention has been described based on a preferred embodiment, but the technical idea of the present invention is not limited thereto, and modifications or changes can be implemented within the scope described in the claims. It is obvious to the user, and such modifications or changes will fall within the scope of the appended claims.

100: nucleic acid extraction cartridge
200: PCR plate
210: body
220: insert
300: temperature control module
310: first heating block
320: second heating block
330: drive module
340: cooling fan unit
350: constant temperature plate
400: horizontal movement drive module
500: scanning module
W: reaction well

Claims (20)

A PCR plate receiving the nucleic acid solution from the nucleic acid extraction cartridge and receiving the dried PCR mixture in the reaction well; And
A temperature control module disposed on one side of the PCR plate, applying different temperatures adjacent to the reaction well, and including a pair of heating blocks capable of horizontal operation and vertical movement operation; and
The temperature control module,
A first heating block provided with a first pressing surface corresponding to the surface of the reaction well and maintained at a first temperature;
A second heating block disposed to be spaced apart from the first heating block, provided with a second pressing surface corresponding to the surface of the reaction well, and maintained at a second temperature; And
Includes; a driving module that implements a horizontal operation or vertical movement operation of the first heating block and the second heating block, and
The driving module,
And a guide member passing through each of the first heating block and the second heating block,
The polymerase chain reaction system, characterized in that the first heating block and the second heating block are moved up and down along the guide member.
The first temperature is a temperature required for thermal denaturation,
The second temperature is a polymerase chain reaction system, characterized in that the temperature required for annealing.
The method of claim 1,
A polymerase chain reaction system comprising: a cooling fan unit that controls heat radiation conduction between the first heating block and the second heating block.
The method of claim 1,
The polymerase chain reaction system, wherein the first heating block and the second heating block cross each other according to an operation of the driving module to move up and down.
The method of claim 1,
At least one side of the first heating block and the second heating block,
A polymerase chain reaction system comprising: a temperature control pattern part implemented on the surface of one side.
The method of claim 1,
The polymerase chain reaction system, wherein the first heating block and the second heating block are maintained at the first temperature and the second temperature, respectively, by a temperature sensor and a heating unit.
delete The method of claim 1,
The polymerase chain reaction system further comprising; an elastic member disposed under the guide member.
The method of claim 1,
A polymerase chain reaction system comprising: a constant temperature plate disposed on the other side of the PCR plate and maintaining the temperature of the PCR plate at the first temperature or the second temperature.
The method of claim 9,
The constant temperature plate,
A first region heated to the first temperature; And
And a second region spaced apart from the first region and heated to the second temperature,
The first pressing surface is disposed to correspond to the upper portion of the first region,
The polymerase chain reaction system, characterized in that the second pressing surface is disposed to correspond to the upper portion of the second region.
The method of claim 9,
The polymerase chain reaction system, characterized in that the temperature control module and the constant temperature plate are implemented integrally with each other through the guide member.
The method of claim 9,
The polymerase chain reaction system further comprising a; horizontal movement driving module for horizontally moving the constant temperature plate to the lower portion of the PCR plate.
The method of claim 10,
The constant temperature plate,
Further comprising a spacer for partitioning the first region and the second region,
The polymerase chain reaction system, characterized in that the first region and the second region are connected to each other based on both ends of the spacer.
The method of claim 10,
The constant temperature plate is a polymerase chain reaction system, characterized in that formed by bonding metal plates corresponding to the first region and the second region in close contact with each of the heating elements and temperature sensors.
The method of claim 12,
The horizontal movement of the constant temperature plate is implemented in a sliding method,
Polymerase chain reaction system, characterized in that the movement in contact with the sliding tape in contact with the side portion of the constant temperature plate.
The method of claim 10,
When the first region is horizontally moved to the bottom of the PCR plate and disposed, the first heating block moves from top to bottom and is pressed to face the top surface of the PCR plate,
When the second region is horizontally moved to the bottom of the PCR plate, the second heating block moves from top to bottom and is pressed to face the top surface of the PCR plate. .
The method of claim 10,
In the case of temperature cycling for the PCR plate,
In order to raise to the first temperature, the first heating block is moved horizontally to face the upper surface of the PCR plate, and after the first area is moved horizontally, the first heating block is moved downward and the PCR plate The lower surface of is pressed in contact with the first region,
In order to lower to the second temperature, the upper surface of the PCR plate is horizontally moved to face the second heating block, and after the second area is horizontally moved, the second heating block is moved down to the PCR plate. The polymerase chain reaction system, characterized in that the lower surface of the polymerase chain reaction system is pressed in contact with the second region.
delete The method of claim 9,
And a scanning module for irradiating light to the PCR plate and scanning light according to the concentration of the reactant amplified in the reaction well.
The method of claim 19,
The constant temperature plate,
A polymerase chain reaction system comprising: a light transmitting part formed in a through structure through which the detection light of the scanning module can pass.

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